PE20190503A1 - NMDA ESPIRO-LACTAM RECEIVER MODULATORS AND USE OF THE SAME - Google Patents

NMDA ESPIRO-LACTAM RECEIVER MODULATORS AND USE OF THE SAME

Info

Publication number
PE20190503A1
PE20190503A1 PE2019000296A PE2019000296A PE20190503A1 PE 20190503 A1 PE20190503 A1 PE 20190503A1 PE 2019000296 A PE2019000296 A PE 2019000296A PE 2019000296 A PE2019000296 A PE 2019000296A PE 20190503 A1 PE20190503 A1 PE 20190503A1
Authority
PE
Peru
Prior art keywords
halogen
independently selected
nmda
alkyl
espiro
Prior art date
Application number
PE2019000296A
Other languages
Spanish (es)
Inventor
M Amin Khan
Original Assignee
Aptinyx Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aptinyx Inc filed Critical Aptinyx Inc
Publication of PE20190503A1 publication Critical patent/PE20190503A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10Spiro-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4747Quinolines; Isoquinolines spiro-condensed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10Spiro-condensed systems

Abstract

Se refiere a un compuesto representado por la formula expuesta, o una sal farmaceuticamente aceptable y/o un estereoisomero del mismo, caracterizado porque: X y Y son NR1 o CR2R2 (uno de estos es NR1); R1 se selecciona de H, alquiloC1-C6, entre otros; q es 0 o 1; r es 1 o 2; R2 se selecciona de forma independiente de H, halogeno, entre otros; R3 se selecciona de H, fenilo, entre otros; R5 se selecciona de forma independiente de H, alquiloC1-C6, entre otros; R6 es 1 o 2 sustituyentes por cada carbono de anillo disponible (se selecciona de halogeno, alquiloC1-C6, entre otros); R7 se selecciona de forma independiente de H, halogeno, entre otros; y R9 se selecciona de forma independiente de H, halogeno, entre otros; y a una formulacion o composicion farmaceutica que comprende al compuesto de la invencion (puede ser su mezcla racemica) junto a un excipiente farmaceuticamente aceptable (segun su via de administracion. Tambien se refiere a metodos de preparacion y de tratamiento (para esto tambien se pueden emplear terapias de combinacion con uno o mas de otros agentes activos). La presente invencion es util para el tratamiento de afecciones tales como depresion y trastornos relacionados mediante la modulacion de la actividad del receptor de N-metil-d-aspartato (NMDA).It refers to a compound represented by the exposed formula, or a pharmaceutically acceptable salt and / or a stereoisomer thereof, characterized in that: X and Y are NR1 or CR2R2 (one of these is NR1); R1 is selected from H, C1-C6 alkyl, among others; q is 0 or 1; r is 1 or 2; R2 is independently selected from H, halogen, among others; R3 is selected from H, phenyl, among others; R5 is independently selected from H, C1-C6 alkyl, among others; R6 is 1 or 2 substituents for each available ring carbon (selected from halogen, C1-C6 alkyl, among others); R7 is independently selected from H, halogen, among others; and R9 is independently selected from H, halogen, among others; and a pharmaceutical formulation or composition comprising the compound of the invention (it can be its racemic mixture) together with a pharmaceutically acceptable excipient (according to its route of administration. It also refers to methods of preparation and treatment (for this they can also be used combination therapies with one or more other active agents.) The present invention is useful for the treatment of conditions such as depression and related disorders by modulating the activity of the N-methyl-d-aspartate receptor (NMDA).

PE2019000296A 2016-08-01 2017-08-01 NMDA ESPIRO-LACTAM RECEIVER MODULATORS AND USE OF THE SAME PE20190503A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662369453P 2016-08-01 2016-08-01

Publications (1)

Publication Number Publication Date
PE20190503A1 true PE20190503A1 (en) 2019-04-10

Family

ID=59582038

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2019000296A PE20190503A1 (en) 2016-08-01 2017-08-01 NMDA ESPIRO-LACTAM RECEIVER MODULATORS AND USE OF THE SAME

Country Status (17)

Country Link
US (3) US11299495B2 (en)
EP (1) EP3490992B1 (en)
JP (2) JP2019527233A (en)
KR (1) KR102465758B1 (en)
CN (1) CN109937204B (en)
AU (2) AU2017306152A1 (en)
BR (1) BR112019001768A2 (en)
CA (1) CA3031537A1 (en)
CL (1) CL2019000248A1 (en)
CO (1) CO2019000945A2 (en)
EA (1) EA201990424A1 (en)
IL (1) IL264514B (en)
MX (1) MX2019001319A (en)
PE (1) PE20190503A1 (en)
PH (1) PH12019500202A1 (en)
SG (2) SG10202101055VA (en)
WO (1) WO2018026779A1 (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101769999B1 (en) 2008-09-18 2017-08-21 노오쓰웨스턴 유니버시티 Nmda receptor modulators and uses thereof
EP3514158B1 (en) 2013-01-29 2022-10-12 Aptinyx Inc. Spiro-lactam nmda receptor modulators and uses thereof
US10918637B2 (en) 2016-08-01 2021-02-16 Aptinyx Inc. Spiro-lactam NMDA receptor modulators and uses thereof
WO2018026779A1 (en) 2016-08-01 2018-02-08 Aptinyx Inc. Spiro-lactam nmda receptor modulators and uses thereof
EP3490994B8 (en) 2016-08-01 2024-03-13 Tenacia Biotechnology (Hong Kong) Co., Limited Spiro-lactam and bis-spiro-lactam nmda receptor modulators and uses thereof
SG11201900558RA (en) 2016-08-01 2019-02-27 Aptinyx Inc Spiro-lactam nmda receptor modulators and uses thereof
WO2018026798A1 (en) 2016-08-01 2018-02-08 Aptinyx Inc. Spiro-lactam nmda modulators and methods of using same
US11578072B2 (en) * 2018-01-31 2023-02-14 Aptinyx Inc. Spiro-lactam NMDA receptor modulators and uses thereof
CN109608460A (en) * 2018-12-17 2019-04-12 上海合全药业股份有限公司 A kind of synthetic method of 1,10- dioxy subunit -2,7- diaza spiro [4.5] decane -7- t-butyl formate
WO2021228123A1 (en) * 2020-05-12 2021-11-18 北京广为医药科技有限公司 Compound for adjusting activity of nmda receptor, and pharmaceutical composition and use thereof
CN114591326B (en) * 2022-02-28 2024-02-27 上海筛杰生物医药有限公司 Intermediate of CCT-251921 and preparation method thereof

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